Non-interventional Surveillance of Effectiveness of Symbicort® Maintenance And Reliever Therapy (Symbicort® SMART) in the Treatment of Moderate and Severe Asthma

NCT00573222 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 330

Last updated 2010-12-01

No results posted yet for this study

Summary

This is a 3-month non-interventional, observational study on patients with moderate and severe asthma.

Conditions

Interventions

DRUG

Symbicort

Sponsors & Collaborators

Principal Investigators

  • Anan Marija Gjurovic · AstraZeneca

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-11-30
Primary Completion
2008-05-31
Completion
2008-05-31

Countries

  • Croatia

Study Locations

More Related Trials

Entities

Diseases
Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00573222 on ClinicalTrials.gov